Controlling electrostatic co-assembly using ion-containing copolymers: From surfactants to nanoparticles

被引:55
作者
Berret, J. -F. [1 ]
机构
[1] Univ Paris 07, CNRS, UMR 7057, F-75205 Paris, France
关键词
POLYION COMPLEX MICELLES; ENTRAPPING ENZYME MOLECULES; OPPOSITELY CHARGED POLYMERS; IRON-OXIDE NANOPARTICLES; BLOCK-COPOLYMERS; MAGNETIC NANOPARTICLES; PHASE-BEHAVIOR; ADSORPTION PROPERTIES; DIBLOCK COPOLYMERS; DNA;
D O I
10.1016/j.cis.2011.01.008
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
In this review, we address the issue of the electrostatic complexation between charged-neutral diblock copolymers and oppositely charged nanocolloids. We show that nanocolloids such as surfactant micelles and iron oxide magnetic nanoparticles share similar properties when mixed with charged-neutral diblocks. Above a critical charge ratio, core-shell hierarchical structures form spontaneously under direct mixing conditions. The core-shell structures are identified by a combination of small-angle scattering techniques and transmission electron microscopy. The formation of multi-level objects is driven by the electrostatic attraction between opposite charges and by the release of the condensed counterions. Alternative mixing processes inspired from molecular biology are also described. The protocols applied here consist in screening the electrostatic interactions of the mixed dispersions, and then removing the salt progressively as an example by dialysis. With these techniques, the oppositely charged species are intimately mixed before they can interact, and their association is monitored by the desalting kinetics. As a result, sphere- and wire-like aggregates with remarkable superparamagnetic and stability properties are obtained. These findings are discussed in the light of a new paradigm which deals with the possibility to use inorganic nanoparticles as building blocks for the design and fabrication of supracolloidal assemblies with enhanced functionalities. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:38 / 48
页数:11
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